HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251516Generated: October 26, 2026
Hydrochloric Acid → 2-Chloro-1-(3,4-difluorophenyl)ethanone
https://huagongshe.com/reaction/251516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | 1,2-Difluorobenzene | HCID 9706 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-1-(3,4-difluorophenyl)ethanone | HCID 2392321 | 80.9% |
Reaction Steps
Aluminium trichloride (210.2 g) was added to 1,2-difluorobenzene (200.0 g) at room temperature. The obtained slurry was heated to 50° C., then chloroacetyl chloride (198.0 g) was added over 50 minutes. The reaction mixture was stirred for an additional 60 minutes, then added slowly to a mixture of ice (786.0 g), water (196.0 g) and 37 wt % hydrochloric acid (297.0 g), during the addition the temperature was kept below 60° C. After the addition, the reaction mixture was heated to 60° C. and the layers separated. The organic layer was washed twice with a 20 w/v % sodium chloride solution (200.0 mL). 2-Chloro-1-(3,4-difluorophenyl)ethanone (270.2 g) was obtained by vacuum distillation of the organic layer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863469B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-b7426b474d3f42bd9d4767851118fb29 |
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| Source note | uspto-grants-2011_01 |
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